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. Author manuscript; available in PMC: 2010 Aug 16.
Published in final edited form as: Cell Biochem Biophys. 2010 Jul;57(2-3):67–76. doi: 10.1007/s12013-010-9084-1

Fig. 7.

Fig. 7

Semi-quantitative RT-PCR analysis of dicer, TIMP-4, and serca-2a. The mRNA from FVB and MMP-9KO cardiomyocytes was isolated and amplified for dicer (a) and TIMP-4 (b) regions. GAPDH (c) was used as loading control. d The bar graph represents real-time PCR amplification of serca-2a in FVB and MMP-9KO cardiomyocytes. GAPDH was used as endogenous control. Each bar represents average ± SD from 5 to 7sets of myocytes preparation. * P < 0.05 compared with FVB myocytes